Exploiting the 3-Aminopropyltriethoxysilane (APTES) autocatalytic nature to create bioconjugated microarrays on hydrogen-passivated porous silicon

TALANTA

卷:177

Article

Coombs, Sidney G.¹  Khodjaniyazova, Sitora¹  Bright, Frank V.¹ 

[1] SUNY Buffalo, Dept Chem, Nat Sci Complex, Buffalo, NY 14260 USA

关键词: Porous silicon;    Microarray;    3-Aminopropyltriethoxysilane;    Photoluminescence;    FT-IR;    Bioconjugation;   

DOI  :  10.1016/j.talanta.2017.09.038

来源: Elsevier

【 摘 要 】

Porous silicon (pSi) based microarrays are attractive because pSi: (i) can be modified in many ways, (ii) possesses a high surface area, and (iii) exhibits strong photoluminescence (PL). These characteristics make pSi-based microarrays candidates for a host of applications including sensing, optoelectronic devices, and photodetectors. Microarray fabrication requires a high-throughput approach to produce chemically modified, spatially isolated spots on a particular substrate. The most stable platforms are characterized by covalent attachment to the substrate. In this paper we exploit the autocatalytic nature of 3-aminopropyltriethoxysilane (APTES) to contact pin-print APTES directly onto as prepared, H-passivated pSi (ap-pSi) without the need for a formal oxidation step. We assess the APTES-derived spots by using PL and Fourier transform infrared spectroscopy (FT-IR) imaging and determine the spot size and spatial homogeneity. All APTES-derived spots exhibited two distinct regions; a silanized core surrounded by an oxidized halo. By decreasing the APTES concentration and increasing the acid concentration, the oxidized halo size decreased by 60%; however, the silanized core diameter remains APTES and acid concentration independent. Bioconjugation can be achieved to all APTES-derived features; however, the highest biomolecule loading was realized by using pure APTES. Together these experiments demonstrate an easy and simple strategy for creating protein microarrays on pSi.

【 授权许可】

Free